[Optimization of Dyeing Wastewater Treatment with New Eco-friendly Polysilicate Ferromanganese].

To improve the efficiency of the removal of dye wastewater, a new type of coagulant "polysilicate ferromanganese (PSFM)" has been synthesized using sodium silicate, ferrous sulfate, and potassium permanganate. Three dyes (direct red, disperse blue, and active yellow) were used for the coagulation tests. The effects of the alkalinity and turbidity on the performance of PSFM were studied. The experimental results show that PSFM performs well with respect to the coagulation of the direct red and disperse blue dyes. The color and TOC removal efficiencies reach 99.2%, 95.4% and 98.5%, and 93.8%, respectively. The coagulation performance is better than that of the conventional coagulants polysilicate iron (PSF), Al2(SO4)3, and FeCl3. The color and TOC removal rates of PSFM for the active yellow dye reach 56% and 51%, respectively. Turbidity has no significant effect on the coagulation efficiency of PSFM. The purification efficiency and alkalinity depend on the amount of dye to be removed. The best alkalinity for the direct red, disperse blue, and active yellow dyes is 50 mg·L-1, 0 mg·L-1, and 75 mg·L-1, respectively. In addition, PSFM has been characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The Zeta potentials of the mixed solutions and flocs during coagulation were also determined. The main indicators of PSFM coagulation are positively charged polynuclear complexes produced by hydrolysis of Fe+ and Mn+ and the bridging polymerization of polysilicon. The adsorption of hydrated manganese dioxide and hydroxyl oxide may also be included.

[Adsorption of Tetracycline on Simulated Suspended Particles in Water].

The mechanism of adsorption of a typical antibiotic (tetracycline, TC) on particles in the aquatic environment and the parameters affecting adsorption were investigated. Experiments were conducted to elucidate the effects of pH and various cation species with different concentrations. The results show that the adsorption of TC on particles is rapid during the first four hours in the mixing stage. The adsorption process becomes slow after the first four hours. The adsorption of TC on particles can be described well by a Langmuir equation. The maximum adsorption of TC on particles occurs at pH 4.5, however it is reduced by strongly acidic (pH<4) or alkaline (pH>9) conditions. Moreover, the adsorption process is also inhibited by various cations (e.g. Na+ and Ca2+) in the range of 0.0001-0.1 mol·L-1 ionic concentrations. A special finding concerns Al3+ ions; at a low concentration of these ions (0-0.0001 mol·L-1) the adsorption of TC on particles improves, whereas at increased concentrations the adsorption is weakened. In summary, an effective removal of the particles is critical to control TC pollution in natural waters because of the rapid adsorption of TC on particles.

[Health risk assessment of heavy metals in typical township water sources in DongjianG River basin].

In order to clarify the distribution characteristics and risk levels of heavy metals in typical drinking water sources of towns in Dongjiang River Basin, several regular water quality indexes as well as concentrations of Fe, Cu, Mn, Zn, As, Cr, Hg, Pb and Cd were analyzed in the 45 random water samples of 9 towns in the study area. The risk assessment was conducted according to different drinking water types using the environmental health risk assessment model recommended by U. S. EPA. The results indicated that the metal carcinogenic risk is relatively high in this area. The highest carcinogenic risk was from Cr in reservoir water, with the risk for adult people reaching 1.14 x 10(-4) x(-1) and the risk of children reaching 2.14 x 10(-4) x a(-1). Total carcinogenic risk of reservoir, river and underground water exceeded the accepted level of 5.0 x 10(5) x a(-1) as suggested by ICRP while all the non-carcinogenic risk levels were within the acceptable range. The primary control sequence of metal pollution in this area was Cr > As > Pb > Fe > Zn; the risk value of different drinking water sources descended in this order: reservoir > river > underground water > mountain spring.

Seasonal variations of chemical and physical characteristics of dissolved organic matter and trihalomethane precursors in a reservoir: a case study.

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during water treatment are of great public health concern. Understanding the seasonal changes in DOM composition and their reactivity in DBP formation could lead to a better treatment of drinking water and a more consistent water quality. DOM from the East-Lake, a reservoir in the south-China, was fractionated and characterized by XAD resin adsorption (RA) and ultrafiltration (UF) techniques during different seasons within a year. The properties of chemical fractions (isolated by RA) appeared more stable than those of physical fractions (separated by UF) throughout the sampling period. The relative contribution of each chemical fraction to the total dissolved organic carbon (DOC), UV(254) absorbance and trihalomethane formation potential (THMFP) remained relatively constant across the sampling period. However, the physical (molecular weight) fractions of the DOM exhibited large seasonal changes in UV(254) and THMFP. Compared to the parameter of DOC, the THMFP and specific THMFP (STHMFP) of either chemical or physical fractions were more variable. In terms of DOC concentration, the hydrophobic acids (HoA) and hydrophilic matter (HiM) dominated in the DOM in most of the seasons; while the components with molecular weight of 10-30 kDa and less than 1 kDa were the predominant physical fractions.

Transformations of particles, metal elements and natural organic matter in different water treatment processes.

Characterizing natural organic matter (NOM), particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Pre-ozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon (GAC) filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant (HPAC) was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.